Chunhua Wang1, Li Song, Ruzhi Zhang, and Fabao Gao
1Department of Radiology, West China Hospital, Chengdu, People's Republic of China
Synopsis
Ex vivo diffusion tensor imaging (DTI) are widely used in experimental
studies for excellent images. The comparison between in vivo and ex vivo DTI has
been conducted without the same scan parameters. We aimed to compare the living
and fixed white and gray matters under the same condition and explore the effects
of coil and signal average. Diffusivities were significant different between living
and fixed brains. Coil and signal average significantly affected the signal-to-noise
ratio of ex vivo white and gray matters. The results indicate that fixation and
MR conditions should be considered in clinical and experimental DTI studies.
PURPOSE: To assess the
effects of fixation, coil and signal average on gray and white matters using diffusion
tensor imaging (DTI).
METHODS: Six
male SD rats underwent DTI MR for brains under conditions of in vivo with
surface coil and 1 signal average (S1), ex vivo with S1 as well as volume coil
with 1 and 4 averages (V1 and V4), and surface coil with 4 averages (S4). The
data collected included mean diffusivity (MD), axial diffusivity (AD), radial
diffusivity (RD), fractional anisotropy (FA), λ2/λ1, λ3/λ1, and λ2/λ3. Comparison
of Signal-to-noise ratio (SNR) were conducted in fixed brains. Regions of
interest (ROIs) included white matters (WMs) of corpus callosum (CC), external
capsule (EC), and internal capsule and cerebral peduncle (ICCP), and gray
matters (GMs) of cortex (CT), hippocampus (HP), and caudate putamen (CU).
RESULTS: The data of
diffusivities are summarized in table 1, 2, and 3. MD, AD, and RD of ex vivo ROIs
with different coils and averages were lower than those of in vivo ROIs (all p < 0.001). Multi-factor ANOVA demonstrated
that fixation significantly affected diffusivities of all ROIs (all
p < 0.001). There were both
significances and nonsignificances in comparisons of FA, λ2/λ1, λ3/λ1, and λ2/λ3
between in vivo and ex vivo from different ROIs. There were significant
differences in SNR of 1 average between surface and volume coils, and in SNR of
surface coil between 1 and 4 averages from all ROIs (all p < 0.05; Table 4). The multi-factor ANOVA determined that coil
and average significantly affected the SNR in all the ROIs.
DISCUSSION: The present study
found diffusivities of brain white and gray matters reduced after fixation,
which is consistent with previous studies (1-3).
The principles involves structural change of proteins, tissue shrinkage, fixation
processes and fixative, and temperature (4-8).
Previous study confirmed the similar SNR in the cartilage with both surface and
volume coils (9). However, we found
higher SNR with surface coil than with volume coil, suggesting there were
different coil effects on SNR in different tissues. Furthermore, there was a
higher SNR from surface coil with 4 averages than with 1 average.
CONCLUSION: Fixation, coil and
signal average affect the DTI values, and need to take into account in clinical
and experimental studies.Acknowledgements
No acknowledgement found.References
1. Sun
SW, Neil JJ, Song SK. Relative indices of water diffusion anisotropy are
equivalent in live and formalin-fixed mouse brains. Magn Reson Med.
2003;50(4):743-748.
2. Rane
S, Duong TQ. Comparison of in vivo and ex vivo diffusion tensor imaging in
rhesus macaques at short and long diffusion times. Open Neuroimag J.
2011;5(172-178.
3. Wu
D, Xu J, McMahon MT et al. In vivo high-resolution diffusion tensor imaging of
the mouse brain. Neuroimage. 2013;83(18-26.
4. Werner
M, Chott A, Fabiano A et al. Effect of formalin tissue fixation and processing
on immunohistochemistry. Am J Surg Pathol. 2000;24(7):1016-1019.
5. Quester
R, Schroder R. The shrinkage of the human brain stem during formalin fixation
and embedding in paraffin. J Neurosci Methods. 1997;75(1):81-89.
6. Wehrl
HF, Bezrukov I, Wiehr S et al. Assessment of murine brain tissue shrinkage
caused by different histological fixatives using magnetic resonance and
computed tomography imaging. Histol Histopathol. 2015;30(5):601-613.
7. Madi
S, Hasan KM, Narayana PA. Diffusion tensor imaging of in vivo and excised rat
spinal cord at 7 T with an icosahedral encoding scheme. Magn Reson Med.
2005;53(1):118-125.
8. Le
Bihan D. Diffusion and perfusion magnetic resonance imaging-applications to
functional MRI. New York: Raven Press. 1995;
9. Bittersohl
B, Huang T, Schneider E et al. High-resolution MRI of the triangular
fibrocartilage complex (TFCC) at 3T: comparison of surface coil and volume
coil. J Magn Reson Imaging. 2007;26(3):701-707.